WDR27
WD repeat-containing protein 27
Also known as: MGC43690, WDR27_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A2RRH5
- Gene
- WDR27
- Ensembl
- ENSG00000184465
- Chromosome
- 6
- Canonical length
- 827 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
This gene encodes a protein with multiple WD repeats. Proteins with these repeats may form scaffolds for protein-protein interaction and play key roles in cell signalling. Alternative splicing results in multiple transcript variants, but the full-length structure of some of these variants cannot be determined. [provided by RefSeq, Nov 2015]
Canonical amino-acid sequenceUniProt
827 residues, UniProt reviewed canonical sequence.
>A2RRH5|WDR27
1 MENPQDIFSS NGGCLSDIVI EKYLVESKES VSHVQLACSM QDCAFPLDGT ELCIWNTKDP
61 SHQLLILRGH HQPITAMAFG NKVNPLLICS ASLDYVIMWN LDECREKVLQ GLVPRGTVMG
121 SLLGKVLCLQ LSLDDHVVAV CAGNKIFMLD IETQAVRAEL QGHLGPVTAV EFCPWRAGTL
181 ISASEDRGFK VWDHCTGSLI YSSSVLSAYP LLSLFIDAES RQLVTGCADG QLWIFSLMDG
241 HHYRRVARVD LRKKTETFST RRVKSGLCSQ PEESQLPSTS ALGKGEQVEV TFPVLRLAPC
301 DLSLIPNSAC GCLSSENTRC VWIGSSVGLF VFNLANLEVE AALYYKDFQS LSILLAGSCA
361 LRNRTADQKV LCLLASLFGG KIAVLEINPA ALVRAQQCPS MGQSLSVPAS SCVLPTSPLY
421 LGIAKEKSTK AASEQRRAAR NVMKDQRLVF HSKVRSSGYA SAPHVTMFSP KTNIKSEGKG
481 SSRSRSSCAR EAYPVECAVP TKPGPQVAAA PTCTRVCCIQ YSGDGQWLAC GLANHLLLVF
541 DASLTGTPAV FSGHDGAVNA VCWSQDRRWL LSAARDGTLR MWSARGAELA LLLGKDMFSK
601 PIQSAQFYYI DAFILLSSGP EFQLLRYHID TCKDEIKRYK QKSKSKLICR LSTTGAVDMT
661 SLSAVNDFYS HIVLAAGRNR TVEVFDLNAG CSAAVIAEAH SRPVHQICQN KGSSFTTQQP
721 QAYNLFLTTA IGDGMRLWDL RTLRCERHFE GHPTRGYPCG IAFSPCGRFA ACGAEDRHAY
781 VYEMGSSTFS HRLAGHTDTV TGVAFNPSAP QLATATLDGK LQLFLAELocalizationUniProt · AlphaFold · HPA
Whether an antibody against WDR27 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.28
- Highest tissue expression
- 7.4 nTPM
Expression across tissuesHPA
Tissue
- thyroid gland: 7.4 nTPM
- testis: 7.3 nTPM
- ovary: 7 nTPM
- cervix: 6.8 nTPM
- fallopian tube: 6.6 nTPM
- endometrium: 6 nTPM
Single-cell type
- distal convoluted tubule cells: 138 nCPM
- renal connecting tubule cells: 113 nCPM
- proximal tubule cells: 107 nCPM
- loop of henle epithelial cells: 104 nCPM
- renal collecting duct principal cells: 91 nCPM
- podocytes: 91 nCPM
Immune cell
- naive CD4 T-cell: 1.6 nTPM
- naive B-cell: 0.9 nTPM
- MAIT T-cell: 0.8 nTPM
- memory CD4 T-cell: 0.5 nTPM
- memory CD8 T-cell: 0.5 nTPM
- eosinophil: 0.4 nTPM
Brain region
- choroid plexus: 17 nTPM
- cerebellum: 10 nTPM
- basal ganglia: 9.7 nTPM
- cerebral cortex: 9.6 nTPM
- hypothalamus: 9.5 nTPM
- medulla oblongata: 9.3 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.89
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.59
- DepMap mean gene effect
- 0.11
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads WDR27 as an antibody target. Whether an autoantibody or antibody against WDR27 could matter depends on whether native WDR27 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
WDR27 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label WDR27 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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